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Clinicopathologic and molecular correlates to neoadjuvant chemotherapy‐induced pathologic response in breast angiosarcoma.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 5, p. 1, doi. 10.1002/gcc.23240
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- Article
Genomic profiling of pleomorphic rhabdomyosarcoma reveals a genomic signature distinct from that of embryonal rhabdomyosarcoma.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 5, p. 1, doi. 10.1002/gcc.23238
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- Article
FGFR1 fusions as a novel molecular driver in rhabdomyosarcoma.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 4, p. 1, doi. 10.1002/gcc.23232
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A phase 2 study of MK‐2206 in patients with incurable adenoid cystic carcinoma (Alliance A091104).
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- Cancer (0008543X), 2024, v. 130, n. 5, p. 702, doi. 10.1002/cncr.35103
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Spindle cell neoplasms with novel LTK fusion – Expanding the spectrum of kinase fusion‐positive soft tissue tumors.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 3, p. 1, doi. 10.1002/gcc.23227
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Epithelioid hemangioendothelioma (EHE) with WWTR1::TFE3 gene fusion, a novel fusion variant.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 2, p. 1, doi. 10.1002/gcc.23226
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CIC-DUX4 Chromatin Profiling Reveals New Epigenetic Dependencies and Actionable Therapeutic Targets in CIC-Rearranged Sarcomas.
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- Cancers, 2024, v. 16, n. 2, p. 457, doi. 10.3390/cancers16020457
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Expanding the molecular landscape of undifferentiated sarcomas of bone with a novel EWSR1‐SSX3 gene fusion.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 1, p. 1, doi. 10.1002/gcc.23215
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Untying the Gordian knot of composite hemangioendothelioma: Discovery of novel fusions.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 1, p. 1, doi. 10.1002/gcc.23198
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When molecular outsmarts morphology: Malignant ossifying fibromyxoid tumors masquerading as osteosarcomas, including a novel CREBZF::PHF1 fusion.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 1, p. 1, doi. 10.1002/gcc.23206
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Complementary value of molecular analysis to expert review in refining classification of uncommon soft tissue tumors.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 1, p. 1, doi. 10.1002/gcc.23196
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Kinase fusion positive intra‐osseous spindle cell tumors: A series of eight cases with review of the literature.
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- Genes, Chromosomes & Cancer, 2024, v. 63, n. 1, p. 1, doi. 10.1002/gcc.23205
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- Article
Novel EWSR1::GFI1B gene fusion in angiofibroma of soft tissue.
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- Histopathology, 2023, v. 83, n. 6, p. 959, doi. 10.1111/his.15044
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- Article
An SRF‐rearranged malignant cellular myoid neoplasm with a novel SRF–MKL2 fusion.
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- Pediatric Blood & Cancer, 2023, v. 70, n. 12, p. 1, doi. 10.1002/pbc.30675
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- Article
Sequential genomic analysis using a multisample/multiplatform approach to better define rhabdomyosarcoma progression and relapse.
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- NPJ Precision Oncology, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41698-023-00445-1
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- Article
Modeling sarcoma relevant translocations using CRISPR‐Cas9 in human embryonic stem derived mesenchymal precursors.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 9, p. 501, doi. 10.1002/gcc.23141
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Distinct genomic landscapes in radiation‐associated angiosarcoma compared with other radiation‐associated sarcoma histologies.
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- Journal of Pathology, 2023, v. 260, n. 4, p. 465, doi. 10.1002/path.6137
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- Article
MED15::TFE3 Renal Cell Carcinomas: Report of Two New Cases and Review of the Literature Confirming Nearly Universal Multilocular Cystic Morphology.
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- International Journal of Surgical Pathology, 2023, v. 31, n. 4, p. 409, doi. 10.1177/10668969221143455
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Malignant undifferentiated epithelioid neoplasms with MAML2 rearrangements: A clinicopathologic study of seven cases demonstrating a heterogenous entity.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 4, p. 191, doi. 10.1002/gcc.23102
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Malignant peripheral nerve sheath tumor in children: A clinicopathologic and molecular study with parallels to the adult counterpart.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 3, p. 131, doi. 10.1002/gcc.23106
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Expanding the molecular spectrum of gene fusions in endometrial stromal sarcoma: Novel subunits of the chromatin remodeling complexes PRC2 and NuA4/TIP60 as alternative fusion partners.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 3, p. 152, doi. 10.1002/gcc.23109
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Generating in vitro models of NTRK-fusion mesenchymal neoplasia as tools for investigating kinase oncogenic activation and response to targeted therapy.
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- Oncogenesis, 2023, v. 12, n. 1, p. 1, doi. 10.1038/s41389-023-00454-6
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ALK‐rearranged Mesenchymal Neoplasms: A Report of 9 cases Further Expanding the Clinicopathologic Spectrum of Emerging Kinase Fusion Positive Group of Tumors.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 2, p. 75, doi. 10.1002/gcc.23097
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RREB1::MRTFB fusion‐positive extra‐glossal mesenchymal neoplasms: A series of five cases expanding their anatomic distribution and highlighting significant morphological and phenotypic diversity.
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- Genes, Chromosomes & Cancer, 2023, v. 62, n. 1, p. 5, doi. 10.1002/gcc.23082
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Recurrent VGLL3 fusions define a distinctive subset of spindle cell rhabdomyosarcoma with an indolent clinical course and striking predilection for the head and neck.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 701, doi. 10.1002/gcc.23083
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ZFP64::NCOA3 gene fusion defines a novel subset of spindle cell rhabdomyosarcoma.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 11, p. 645, doi. 10.1002/gcc.23052
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Mesenchymal chondrosarcoma of the head and neck with HEY1::NCOA2 fusion: A clinicopathologic and molecular study of 13 cases with emphasis on diagnostic pitfalls.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 11, p. 670, doi. 10.1002/gcc.23075
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EWSR1::YY1 fusion positive peritoneal epithelioid mesothelioma harbors mesothelioma epigenetic signature: Report of 3 cases in support of an emerging entity.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 10, p. 592, doi. 10.1002/gcc.23074
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An international working group consensus report for the prioritization of molecular biomarkers for Ewing sarcoma.
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- NPJ Precision Oncology, 2022, v. 6, n. 1, p. 1, doi. 10.1038/s41698-022-00307-2
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NUTM1‐fusion positive malignant neoplasms of the genitourinary tract: A report of six cases highlighting involvement of unusual anatomic locations and histologic heterogeneity.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 9, p. 542, doi. 10.1002/gcc.23046
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Primary renal sarcoma with SS18::POU5F1 gene fusion.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 9, p. 572, doi. 10.1002/gcc.23053
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A novel WWTR1::AFF2 fusion in an intra‐abdominal soft tissue sarcoma with associated endometriosis.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 8, p. 497, doi. 10.1002/gcc.23045
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Ewing sarcoma and related FET family translocation‐associated round cell tumors: A century of clinical and scientific progress.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 8, p. 509, doi. 10.1002/gcc.23050
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FGFR2::TACC2 fusion as a novel KIT‐independent mechanism of targeted therapy failure in a multidrug‐resistant gastrointestinal stromal tumor.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 7, p. 412, doi. 10.1002/gcc.23030
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Expanding the spectrum of mesenchymal neoplasms with NR1D1‐rearrangement.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 7, p. 420, doi. 10.1002/gcc.23032
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Clinical sequencing of soft tissue and bone sarcomas delineates diverse genomic landscapes and potential therapeutic targets.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30453-x
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Clinical sequencing of soft tissue and bone sarcomas delineates diverse genomic landscapes and potential therapeutic targets.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30453-x
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- Article
Recurrent PTBP1::MAML2 fusions in composite hemangioendothelioma with neuroendocrine differentiation: A report of two cases involving neck lymph nodes.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 4, p. 187, doi. 10.1002/gcc.23017
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- Article
Neuregulin 1 (NRG1) fusion‐positive high‐grade spindle cell sarcoma: A distinct group of soft tissue tumors with metastatic potential.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 3, p. 123, doi. 10.1002/gcc.23008
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- Article
Clinicopathologic and survival correlates of embryonal rhabdomyosarcoma driven by RAS/RAF mutations.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 3, p. 131, doi. 10.1002/gcc.23010
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- Article
Low‐grade endometrial stromal sarcoma‐like tumors in male with JAZF1 gene fusions.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 2, p. 63, doi. 10.1002/gcc.23003
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The genetics of vascular tumours: an update.
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- Histopathology, 2022, v. 80, n. 1, p. 19, doi. 10.1111/his.14458
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Gastrointestinal stromal tumors with BRAF gene fusions. A report of two cases showing low or absent KIT expression resulting in diagnostic pitfalls.
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- Genes, Chromosomes & Cancer, 2021, v. 60, n. 12, p. 789, doi. 10.1002/gcc.22991
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A unique epithelioid vascular neoplasm of bone characterized by EWSR1/FUS‐NFATC1/2 fusions.
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- Genes, Chromosomes & Cancer, 2021, v. 60, n. 11, p. 762, doi. 10.1002/gcc.22984
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The impact of MYC gene amplification on the clinicopathological features and prognosis of radiation‐associated angiosarcomas of the breast.
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- Histopathology, 2021, v. 79, n. 5, p. 836, doi. 10.1111/his.14433
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Case Report: Response to Regional Melphalan via Limb Infusion and Systemic PD1 Blockade in Recurrent Myxofibrosarcoma: A Report of 2 Cases.
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- Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.725484
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Targeted RNA sequencing in the routine clinical detection of fusion genes in salivary gland tumors.
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- Genes, Chromosomes & Cancer, 2021, v. 60, n. 10, p. 695, doi. 10.1002/gcc.22979
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PLAG1‐rearrangment in a uterine leiomyosarcoma with myxoid stroma and heterologous differentiation.
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- Genes, Chromosomes & Cancer, 2021, v. 60, n. 10, p. 713, doi. 10.1002/gcc.22980
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Sarcomas with sclerotic epithelioid phenotype harboring novel EWSR1‐SSX1 fusions.
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- Genes, Chromosomes & Cancer, 2021, v. 60, n. 9, p. 616, doi. 10.1002/gcc.22970
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Head and neck rhabdomyosarcoma with TFCP2 fusions and ALK overexpression: a clinicopathological and molecular analysis of 11 cases.
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- Histopathology, 2021, v. 79, n. 3, p. 347, doi. 10.1111/his.14323
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